1961
DOI: 10.1039/jr9610004604
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901. Ferrocene derivatives. Part IX. Some disubstituted derivatives

Abstract: Novel preparations of dimethyl ferrocene-1 , 1'-dicarboxylate, 1,l '-bis-(dimethylaminomethyl) ferrocene, ferrocene-1 , 1'-dicarboxyaldehyde, and 1,l'dicyanoferrocene are described. Some reactions of ferrocene-mono-and -dicarboxyaldehyde are reported.

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Cited by 63 publications
(12 citation statements)
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“…A signal due to CeP of fc is obscured by the solvent resonance while the 13 C due to solvent were not observed due to their poor intensities. EI MS: m/z (relative abundance) 414 (28) (23), 170 (24), 164 (18), 146 (7), 115 (7), 80 (10), 72 (11), 56 (14). HR MS (EI) calc.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…A signal due to CeP of fc is obscured by the solvent resonance while the 13 C due to solvent were not observed due to their poor intensities. EI MS: m/z (relative abundance) 414 (28) (23), 170 (24), 164 (18), 146 (7), 115 (7), 80 (10), 72 (11), 56 (14). HR MS (EI) calc.…”
Section: Methodsmentioning
confidence: 99%
“…In contrast, hydrazide 2 (Scheme 2) was prepared similarly to its non-phosphinylated counterpart (FcCONHNH 2 ) [10] by reacting Hdpf methyl ester (Medpf) [6a] with hydrazine hydrate in refluxing methanol. However, unlike the efficient synthesis of FcCONHNH 2 , the starting Hdpf ester was converted to 2 only partially while the rest remained unchanged (isolated yield of 2: 46%, 86% based on unrecovered Medpf).…”
Section: Preparation and Characterization Of The Ligandsmentioning
confidence: 99%
“…The reaction was diluted with CH 2 Cl 2 and washed (3×) with saturated NaHCO 3 . The organic phase was dried (MgSO 4 ), concentrated, and purified by flash column chromatography (4:1 hexane:ethyl acetate) to give 1 g (60%) of 1,1‘-bis(carbomethoxy)ferrocene …”
Section: Methodsmentioning
confidence: 99%
“…1 Compounds 1 can be prepared by Wittig reaction using ferrocenyl compounds either as carbonyl components or as ylide precursors [17][18][19][20][21] although this way often leads to mixtures of (E)-and (Z)-isomers. Other synthetic methods for 1 involve Heck coupling reaction [22,23], olefin cross-methatesis [24], McMurry reductive coupling of ferrocenyl carbonyl compounds [15,16] and samarium diiodide-promoted condensation of these compounds with benzyl bromides [25].…”
Section: Ar(h)mentioning
confidence: 99%